A. Weindl

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

J.-M. Lee, E.M. Ramos, J.-H. Lee et al. · Neurology · 2012 · 391 citations · Full text

Life Sciences, Genetics, Neurology +15

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Projections from the parvocellular vasopressin‐ and neurophysin‐containing neurons of the suprachiasmatic nucleus

Michael V. Sofroniew, A. Weindl · American Journal of Anatomy · 1978 · 311 citations

Medicine, Anatomy, Neuroscience +9

Changes of NMDA Receptor Subunit (NR1, NR2B) and Glutamate Transporter (GLT1) mRNA Expression in Huntingtonʼs Disease—An In Situ Hybridization Study

Thomas Arzberger, K Krampfl, Susanne Leimgruber et al. · Journal of Neuropathology & Experimental Neurology · 1997 · 227 citations · Full text

Medicine, Neurobiology, Neuroscience +15

Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: A neuropsychological and voxel-based morphometric study

Alexander Peinemann, Sabine Schuller, Corina Pohl et al. · Journal of the Neurological Sciences · 2005 · 185 citations

Life Sciences, Neurology, Neuroscience +13